基本信息
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Career Trajectory
Bio
General Research Area: Ubiquitin Biology and Cell Signalling
The Ubiquitin Biology group at SGC Toronto focuses on understanding the structure, function, specificity, and enzymatic mechanism of E3 ubiquitin ligases and deubiquitinases(DUBs), including key enzymes involved in histone (de-)ubiquitylation and sumoylation. Particularly we are interested in the substrate recognition domains of Ring-inBetween-Ring type, HECT-type E3 ligases, and ubiquitin-specific proteases besides their catalytic domains. These families of proteins have been directly implicated in many human diseases like autism, cancer diabetes, leukemia, allergy, and etc. We are also interested in some guanine nucleotide exchange factors (GEFs) that share common domains ubiquitin ligases or DUBs, in particular the beta-propeller fold domains that are known to modulate protein-protein interaction.
We utilize the SGC’s established high-throughput structural biology platform for protein production, structure determination and biochemical assays to probe the function of these enzymes. We also collaborate with internal and external groups to identify small molecule compounds and biomolecules (ubiquitin variants) that will alter the activity of disease-related ligases and proteases.
The Ubiquitin Biology group at SGC Toronto focuses on understanding the structure, function, specificity, and enzymatic mechanism of E3 ubiquitin ligases and deubiquitinases(DUBs), including key enzymes involved in histone (de-)ubiquitylation and sumoylation. Particularly we are interested in the substrate recognition domains of Ring-inBetween-Ring type, HECT-type E3 ligases, and ubiquitin-specific proteases besides their catalytic domains. These families of proteins have been directly implicated in many human diseases like autism, cancer diabetes, leukemia, allergy, and etc. We are also interested in some guanine nucleotide exchange factors (GEFs) that share common domains ubiquitin ligases or DUBs, in particular the beta-propeller fold domains that are known to modulate protein-protein interaction.
We utilize the SGC’s established high-throughput structural biology platform for protein production, structure determination and biochemical assays to probe the function of these enzymes. We also collaborate with internal and external groups to identify small molecule compounds and biomolecules (ubiquitin variants) that will alter the activity of disease-related ligases and proteases.
Research Interests
Papers共 83 篇Author StatisticsCo-AuthorSimilar Experts
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Brayden LaBute,Jackie Fong, Farinaz Ziaee, Robert Gombar,Mathew Stover, Terry Beaudin, Maria Badalova,Qiudi Geng,Ryland Corchis-Scott, Ana Podadera, Kyle Lago, ZhenHuan Xu, Fievel Lim, Felix Chiu, Minghua Fu, Xiaofeng Nie, Yuanmin Wu, Corrina Quan,Caroline Hamm,R. Michael McKay,Kenneth Ng,Lisa A. Porter,Yufeng Tong
Cody Caba, Megan Black, Yujue Liu,Ashley A. DaDalt, Josh Mallare,Lixin Fan,Rachel J. Harding, Yun-Xing Wang,Panayiotis O. Vacratsis,Rui Huang,Zhihao Zhuang,Yufeng Tong
JOURNAL OF BIOLOGICAL CHEMISTRYno. 10 (2024)
Ryland Corchis-Scott,Qiudi Geng, Abdul Monem Al Riahi, Amr Labak, Ana Podadera,Kenneth K. S. Ng,Lisa A. Porter,Yufeng Tong,Jess C. Dixon, Sherri Lynne Menard,Rajesh Seth,R. Michael Mckay
Frontiers in public health (2023): 1139423-1139423
Cellsno. 6 (2023): 886
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Nastaran Yousefi,Cody Caba,Anita Hu,Madison Mooney,Song Zhang, Alexander D. Agostinis,Mitra Mirhassani,M. Jalal Ahamed,Yufeng Tong,Simon Rondeau-Gagne
ACS APPLIED ELECTRONIC MATERIALSno. 10 (2022): 4972-4981
Biomoleculesno. 5 (2022): 703
R. Corchis-Scott, Q. Geng,R. Seth, R. Ray, M. Beg,N. Biswas, L. Charron,K. G. Drouillard, R. D'Souza, D. D. Heath, C. Houser, F. Lawal, J. McGinlay, S. L. Menard,L. A. Porter, D. Rawlings,Y. Tong, M. L. Scholl,K. W. M. Siu,C. G. Weisener,S. W. Wilhelm,R. M. L. McKay
medRxiv (2021)
Biomolecular NMR assignmentsno. 1 (2021): 179-179
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Author Statistics
#Papers: 82
#Citation: 2150
H-Index: 28
G-Index: 45
Sociability: 6
Diversity: 3
Activity: 6
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